Search results for "organometalli"

showing 10 items of 395 documents

Development of trackable metal-based drugs: new generation of therapeutic agents

2016

International audience; In medicinal chemistry, the aim is not only to conceive ever more efficient molecules, but also to understand their mechanism of action. In very recent years, a new promising strategy was developed to tackle this issue: the conception of trackable therapeutic agents. Metal-based drugs are ideal to exploit this expanding area of research.

Diagnostic ImagingExploitTheranostic NanomedicineComputer scienceNanotechnologyphosphine-porphyrinpotential anticancer agents[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesin-vivo[ CHIM ] Chemical SciencesTheranostic NanomedicineInorganic Chemistrytheranostic agentsplatinum(ii) complexesorganometallic compoundsAnimals[CHIM]Chemical Sciences010405 organic chemistry[ CHIM.INOR ] Chemical Sciences/Inorganic chemistry0104 chemical sciences3. Good healthcancer-cellsRisk analysis (engineering)photodynamic therapycytotoxic propertiesDrug Designheterocyclic carbene complexes
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Ligand effects on the structures and magnetic properties of tricyanomethanide-containing copper(II) complexes.

2007

The preparation, crystal structure and magnetic properties of four heteroleptic copper(II) complexes with the tricyanomethanide (tcm(-)) and the heterocyclic nitrogen donors 3,6-bis(2-pyridyl)pyridazine (dppn), 2,5-bis(2-pyridyl)pyrazine (2,5-dpp), 2,3-bis(2-pyridyl)pyrazine (2,3-dpp) and 2,3-bis(2-pyridyl)quinoxaline (2,3-dpq) are reported, {[Cu(2)(dppn)(OH)(tcm)(2)] x tcm}(n) (1), {[Cu(2,5-dpp)(tcm)] x tcm}(n) (2), {[Cu(2)(2,3-dpp)(2)(tcm)(3)(H(2)O)(0.5)] x tcm x 0.5H(2)O}(n) (3) and [Cu(2,3-dpq)(tcm)(2)](n) (4). 1 has a ladder-like structure with single mu-1,5-tcm ligands forming the sides and a bis-bidentate dppn and a single mu-hydroxo providing the rung. Each copper atom in 1 exhibits…

DiazineModels MolecularDenticityPyrazineMolecular StructureSpectrophotometry InfraredStereochemistryLigandTemperatureCrystal structureCrystallography X-RayLigandsSquare pyramidal molecular geometryInorganic ChemistryPyridazineTrigonal bipyramidal molecular geometrychemistry.chemical_compoundCrystallographyMagneticschemistryNitrilesOrganometallic CompoundsCopperDalton transactions (Cambridge, England : 2003)
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Ferromagnetic dinuclear mixed-valence Mn(II)/Mn(III) complexes: building blocks for the higher nuclearity complexes. structure, magnetic properties, …

2013

A series of six mixed-valence Mn(II)/Mn(III) dinuclear complexes were synthesized and characterized by X-ray diffraction. The reactivity of the complexes was surveyed, and structures of three additional trinuclear mixed-valence Mn(III)/Mn(II)/Mn(III) species were resolved. The magnetic properties of the complexes were studied in detail both experimentally and theoretically. All dinuclear complexes show ferromagnetic intramolecular interactions, which were justified on the basis of the electronic structures of the Mn(II) and Mn(III) ions. The large Mn(II)-O-Mn(III) bond angle and small distortion of the Mn(II) cation from the ideal square pyramidal geometry were shown to enhance the ferromag…

DiffractionModels MolecularManganeseValence (chemistry)Molecular StructureChemistryInorganic ChemistryCrystallographyMagnetic FieldsFerromagnetismComputational chemistryMagnetsOrganometallic CompoundsQuantum TheoryDensity functional theoryPhysical and Theoretical Chemistryta116Inorganic chemistry
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Cryogenic 35GHz pulse ENDOR probehead accommodating large sample sizes: Performance and applications.

2009

The construction and performance of a cryogenic 35GHz pulse electron nuclear double resonance (ENDOR) probehead for large samples is presented. The resonator is based on a rectangular TE(102) cavity in which the radio frequency (rf) B(2)-field is generated by a two turn saddle ENDOR coil crossing the resonator along the sample axis with minimal distance to the sample tube. An rf power efficiency factor is used to define the B(2)-field strength per square-root of the transmitted rf power over the frequency range 2-180MHz. The distributions of the microwave B(1)- and E(1)-field, and the rf B(2)-field are investigated by electromagnetic field calculations. All dielectrics, the sample tube, and…

Electromagnetic fieldNuclear and High Energy PhysicsIndolesPorphyrinsLarge sample resonatorGlycineBiophysicsAnalytical chemistryIsoindolesPulse EPRHeliumBiochemistryResonatorElectromagnetic FieldsOpticsQ-band probeheadMetalloproteinsOrganometallic CompoundsComputer SimulationElectron nuclear double resonanceChemistryPulsed EPRbusiness.industryRF power amplifierElectron Spin Resonance SpectroscopyENDORCondensed Matter PhysicsSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Cold TemperatureCoalENDOR resonatorElectromagnetic coilRadio frequencybusinessAlgorithmsMicrowaveJournal of magnetic resonance (San Diego, Calif. : 1997)
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Fabrication of cobalt and cobalt oxide/graphene composites: towards high-performance anode materials for lithium ion batteries.

2010

Energy-Generating ResourcesFabricationMaterials scienceIndolesLithium vanadium phosphate batteryGeneral Chemical EngineeringInorganic chemistrychemistry.chemical_elementLithiumElectrochemistryMicroscopy Atomic Forcelaw.inventionMicroscopy Electron TransmissionlawOrganometallic CompoundsEnvironmental ChemistryGeneral Materials ScienceCobalt oxideElectrodesGrapheneOxidesCobaltCarbonAnodeGeneral EnergychemistryLithiumCobaltChemSusChem
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Antibacterial studies, DNA oxidative cleavage, and crystal structures of Cu(II) and Co(II) complexes with two quinolone family members, ciprofloxacin…

2005

Nine coordination compounds of Cu(II) and Co(II) with Ciprofloxacin (HCp) and Enoxacin (HEx) as ligands have been prepared and characterized. Single crystal structural determinations of [Cu(HCp)2(ClO4)2].6H2O (1) and [Co(HEx)2(Ex)]Cl.2CH(3)OH.12H2O (4) are reported. The crystal of 1 is composed of [Cu(HCp)2(ClO4)2] units with the two perchlorate anions semicoordinated, and uncoordinated water molecules. The copper ion, at a crystallographic inversion centre, is in a tetragonally distorted octahedral environment. The structure of 4 consists of cationic monomeric [Co(HEx)2(Ex)]+ units, chloride anions, and uncoordinated methanol and water molecules. The complex is six-coordinate, with a sligh…

EnoxacinStereochemistryCrystal structureQuinolonesCrystallography X-RayGram-Positive BacteriaLigandsBiochemistryCoordination complexInorganic Chemistrychemistry.chemical_compoundPerchlorateAnti-Infective AgentsCiprofloxacinCationsGram-Negative BacteriaOrganometallic CompoundsEnoxacinmedicineMoleculeCiprofloxacin HydrochlorideBond cleavageElectrophoresis Agar Gelchemistry.chemical_classificationMolecular StructureCobaltDNAMonomerchemistryOxidation-ReductionCoppermedicine.drugJournal of Inorganic Biochemistry
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Titanium and vanadium catalysts with oxazoline ligands for ethylene-norbornene (co)polymerization

2018

A series of catalysts, (Py-ox)TiCl4, (Py-box)TiCl4, (Py-ox)VCl3, (Py-box)VCl3, SIL/(Py-ox)VCl3, SIL/(Py-box)VCl3, with 2-(1,3-oxazolin-2-yl)pyridine (Py-ox) and 2,6-bis(1,3-oxazolin-2-yl)pyridine (Py-box) ligands, silica support modified by 1-[3-(triethoxysilyl)propyl]pyridinium ethylchloroaluminate ionic liquid (SIL), activated by AlEt2Cl, AlEtCl2, and methylaluminoxane (MMAO) were studied in ethylene polymerization and ethylene-norbornene copolymerization. Single-crystal X-ray diffraction is given for both Py-ox and Py-box. The complexation was confirmed by NMR and ESI-MS methods. All complexes were found to be active in ethylene polymerization with better performance of the vanadium cata…

EthylenePolymers and Plastics010405 organic chemistryOrganic ChemistryMethylaluminoxaneGeneral Physics and AstronomynorbornenePolyethyleneoxazoline ligands010402 general chemistry01 natural sciences0104 chemical sciencesIonic liquidschemistry.chemical_compoundchemistryPolymerizationorganometallic catalystsPolymer chemistryPyridineMaterials ChemistryCopolymercopolymersethylenePyridiniumNorborneneEuropean Polymer Journal
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Counterintuitive Mechanisms of the Addition of Hydrogen and Simple Olefins to Heavy Group 13 Alkene Analogues

2013

The mechanism of the reaction of olefins and hydrogen with dimetallenes ArMMAr (Ar = aromatic group; M = Al or Ga) was studied by density functional theory calculations and experimental methods. The digallenes, for which the most experimental data are available, are extensively dissociated to gallanediyl monomers, :GaAr, in hydrocarbon solution, but the calculations and experimental data showed also that they react with simple olefins, such as ethylene, as intact ArGaGaAr dimers via stepwise [2 + 2 + 2] cycloadditions due to their considerably lower activation barriers vis-à-vis the gallanediyl monomers, :GaAr. This pathway was preferred over the [2 + 2] cycloaddition of olefin to monomeric…

EthyleneStereochemistryGalliumAlkenesBiochemistryMedicinal chemistryCatalysisPropenechemistry.chemical_compoundColloid and Surface ChemistryOrganometallic CompoundsSinglet stateta116chemistry.chemical_classificationOlefin fiberDiradicalChemistryAlkeneGeneral ChemistryCycloadditionCyclizationYield (chemistry)Quantum TheoryCyclobutanesAluminumHydrogenJournal of the American Chemical Society
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Controlled solution-based fabrication of perovskite thin films directly on conductive substrate

2021

Abstract Organometallic perovskites are one of the most investigated materials for high-efficiency thin-film devices to convert solar energy and supply energy. In particular, methylammonium lead iodide has been used to realize thin-film perovskite solar cells, achieving an efficiency higher than 20%. Different fabrication procedures based on the spin-coating technique have been proposed, which do not ensure homogenous morphologies. In this work, we present a scalable process to fabricate methylammonium lead iodide thin films directly on conductive substrates, consisting of electrodeposition and two subsequent chemical conversions. A thorough investigation of the morphological, structural an…

FabricationMaterials scienceAbsorption spectroscopyChemical conversion Electrodeposition Organometallic perovskite Solar cell Thin filmIodide02 engineering and technologySubstrate (electronics)01 natural sciences0103 physical sciencesSettore ING-IND/17 - Impianti Industriali MeccaniciMaterials ChemistryThin filmAbsorption (electromagnetic radiation)Perovskite (structure)010302 applied physicschemistry.chemical_classificationbusiness.industrySettore FIS/01 - Fisica SperimentaleMetals and AlloysSurfaces and Interfaces021001 nanoscience & nanotechnologySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSettore ING-IND/23 - Chimica Fisica ApplicatachemistryOptoelectronics0210 nano-technologybusinessLayer (electronics)
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Metal-organic magnets with large coercivity and ordering temperatures up to 242°C.

2020

International audience; Magnets derived from inorganic materials (e.g., oxides, rare-earth–based, and intermetallic compounds) are key components of modern technological applications. Despite considerable success in a broad range of applications, these inorganic magnets suffer several drawbacks, including energetically expensive fabrication, limited availability of certain constituent elements, high density, and poor scope for chemical tunability. A promising design strategy for next-generation magnets relies on the versatile coordination chemistry of abundant metal ions and inexpensive organic ligands. Following this approach, we report the general, simple, and efficient synthesis of light…

FabricationMaterials sciencemagneettiset ominaisuudetPyrazineMetal ions in aqueous solutionmagneetitIntermetallicNanotechnology02 engineering and technologyorganometalliyhdisteet010402 general chemistrylarge coercivity7. Clean energy01 natural sciencesordering temperaturesCoordination complexchemistry.chemical_compoundMoleculechemistry.chemical_classificationMultidisciplinarymetal-organic magnets[CHIM.MATE]Chemical Sciences/Material chemistrykompleksiyhdisteetCoercivity021001 nanoscience & nanotechnologykiteet0104 chemical scienceschemistryMagnetlämpötila0210 nano-technologyScience (New York, N.Y.)
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